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Lista de obras de Muin J. Khoury

"Drivers" of translational cancer epidemiology in the 21st century: needs and opportunities

artículo científico publicado en 2013

(Mis)classifying limb deficiencies: Reply to "Academicians are more likely to share each other's toothbrush than each other's nomenclature (Cohen, 1982)".

artículo científico publicado en 1998

2012 highlights in translational 'omics

artículo científico publicado en 2013

5,10 Methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects

artículo científico publicado en 1996

A Hardy-Weinberg equilibrium test for analyzing population genetic surveys with complex sample designs.

artículo científico publicado en 2010

A case-control study of maternal alcohol consumption and intrauterine growth retardation

artículo científico publicado en 2001

A critical appraisal of the scientific basis of commercial genomic profiles used to assess health risks and personalize health interventions

artículo científico publicado en 2008

A decade of public health genomics in the United States: centers for disease control and prevention 1997-2007.

artículo científico publicado en 2008

A genetic test registry: bringing credible and actionable data together

artículo científico publicado en 2009

A health services research agenda for cellular, molecular and genomic technologies in cancer care

artículo científico publicado en 2009

A knowledge base for tracking the impact of genomics on population health

artículo científico publicado en 2016

A navigator for human genome epidemiology.

artículo científico publicado en 2008

A network of investigator networks in human genome epidemiology

artículo científico publicado en 2005

A population approach to precision medicine

artículo científico publicado en 2012

A population study of the VACTERL association: evidence for its etiologic heterogeneity

artículo científico publicado en 1983

A primer series on -omic technologies for the practice of epidemiology

artículo científico publicado en 2014

A proposed approach to accelerate evidence generation for genomic-based technologies in the context of a learning health system

artículo científico

A public health approach to pharmacogenomics and gene-based diagnostic tests

artículo científico publicado en 2006

A public health perspective on a national precision medicine cohort: balancing long-term knowledge generation with early health benefit

artículo científico publicado en 2015

A reality check for personalized medicine

artículo científico publicado en 2010

A road map for efficient and reliable human genome epidemiology

artículo científico publicado en 2006

A systematic review of cancer GWAS and candidate gene meta-analyses reveals limited overlap but similar effect sizes

artículo científico publicado en 2013

Accuracy of self-reported family history is strongly influenced by the accuracy of self-reported personal health status of relatives

artículo científico publicado en 2011

Acute intraoperative heparin-induced thrombocytopenia (HIT) and thrombosis during coronary artery bypass grafting: Two case reports providing evidence for the role of preoperative LMWH in triggering sensitization

artículo científico publicado en 2016

Adolescents with severe obesity: outcomes of participation in an intensive obesity management programme

artículo científico publicado en 2014

Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of chromosomal error: a population-based study.

artículo científico publicado en 1996

Age at onset of genetic diseases: an application for Sartwell's model of the distribution of incubation periods ⬇️

artículo científico publicado el 1 de mayo de 1981

Alpha 1-antitrypsin deficiency deaths in the United States from 1979-1991. An analysis using multiple-cause mortality data

artículo científico publicado en 1996

An action plan for translating cancer survivorship research into care

artículo científico publicado en 2014

An automatic method to generate domain-specific investigator networks using PubMed abstracts

artículo científico publicado en 2007

An empirical comparison of meta-analyses of published gene-disease associations versus consortium analyses

artículo científico publicado en 2009

An epidemiologic approach to ecogenetics

artículo científico publicado en 1988

An epidemiologic approach to the evaluation of the effect of inbreeding on prereproductive mortality

artículo científico publicado en 1987

An epidemiologic assessment of genomic profiling for measuring susceptibility to common diseases and targeting interventions

artículo científico publicado en 2004

An open source infrastructure for managing knowledge and finding potential collaborators in a domain-specific subset of PubMed, with an example from human genome epidemiology

artículo científico publicado en 2007

An overview of recommendations and translational milestones for genomic tests in cancer

artículo científico publicado en 2015

Application of population screening principles to genetic screening for adult-onset conditions

artículo científico publicado en 2001

Application of support vector machine modeling for prediction of common diseases: the case of diabetes and pre-diabetes

artículo científico publicado en 2010

Applications of the case-control method in genetic epidemiology

artículo científico publicado en 1994

Applications of the concept of attributable fraction in medical genetics

artículo científico publicado en 1991

Applying public health strategies to primary immunodeficiency diseases: a potential approach to genetic disorders

artículo científico publicado en 2004

Are offspring of women with hereditary hematologic disorders at increased risk of congenital cardiovascular malformations? ⬇️

artículo científico publicado el 1 de enero de 1991

Are randomized trials obsolete or more important than ever in the genomic era?

artículo científico publicado en 2013

Assessing causal relationships in genomics: From Bradford-Hill criteria to complex gene-environment interactions and directed acyclic graphs

artículo científico publicado en 2011

Assessing value in biomedical research: the PQRST of appraisal and reward

artículo científico publicado en 2014

Assessment of cumulative evidence on genetic associations: interim guidelines

artículo científico publicado en 2007

Association of childhood rhabdomyosarcoma with neurofibromatosis type I and birth defects

artículo científico publicado en 1995

Awareness and use of direct-to-consumer nutrigenomic tests, United States, 2006.

artículo científico publicado en 2007

Awareness and utilization of BRCA1/2 testing among U.S. primary care physicians

artículo científico publicado en 2011

BRCA Genetic Testing and Receipt of Preventive Interventions Among Women Aged 18-64 Years with Employer-Sponsored Health Insurance in Nonmetropolitan and Metropolitan Areas - United States, 2009-2014.

artículo científico publicado en 2017

BRCA1 and BRCA2 gene mutations and risk of breast cancer. Public health perspectives

artículo científico publicado en 1999

Beyond base pairs to bedside: a population perspective on how genomics can improve health

artículo científico publicado en 2012

Beyond public health genomics: proposals from an international working group

artículo científico publicado en 2014

Bias associated with study protocols in epidemiologic studies of disease familial aggregation.

artículo científico publicado en 2000

Bias in using family history as a risk factor in case-control studies of disease.

artículo científico publicado en 1995

Building a knowledge base on genetic variation and cancer risk through field synopses.

artículo científico publicado en 2008

Building the evidence base for decision making in cancer genomic medicine using comparative effectiveness research

artículo científico publicado en 2012

CDC Grand Rounds: Family History and Genomics as Tools for Cancer Prevention and Control

artículo científico publicado en 2016

Can familial aggregation of disease be explained by familial aggregation of environmental risk factors?

artículo científico publicado en 1988

Can family history be used as a tool for public health and preventive medicine?

article

Can maternal risk factors influence the presence of major birth defects in infants with Down syndrome?

artículo científico publicado en 1992

Cancer GAMAdb: database of cancer genetic associations from meta-analyses and genome-wide association studies

artículo científico publicado en 2011

Cancer pharmacogenomics and pharmacoepidemiology: setting a research agenda to accelerate translation

artículo científico publicado en 2010

Cancer screening and genetics: a tale of two paradigms

artículo científico publicado en 2014

Cascade Screening for Familial Hypercholesterolemia and the Use of Genetic Testing.

artículo científico publicado en 2017

Case-only design to measure gene-gene interaction.

artículo científico publicado en 1999

Case-parental control method in the search for disease-susceptibility genes

artículo científico publicado en 1994

Challenges in communicating genetics: a public health approach

article

Challenges of translating genetic tests into clinical and public health practice

artículo científico publicado en 2009

Charting a future for epidemiologic training

artículo científico publicado en 2015

Chorionic villus sampling and transverse digital deficiencies: evidence for anatomic and gestational-age specificity of the digital deficiencies in two studies

artículo científico publicado en 1996

Clinical utility of genetic and genomic services: context matters

artículo científico publicado en 2015

Clinical-epidemiologic assessment of pattern of birth defects associated with human teratogens: application to diabetic embryopathy

artículo científico publicado en 1989

Cocaine and single ventricle: a population study

artículo científico

Collaborative biomedicine in the age of big data: the case of cancer

artículo científico publicado en 2014

Collaborative cancer epidemiology in the 21st century: the model of cancer consortia

artículo científico publicado en 2013

Combined anti-inflammatory tritherapy using a novel small interfering RNA lipoplex successfully prevents and cures mice of arthritis.

artículo científico publicado en 2007

Combining molecular and genetic data from different sources

artículo científico publicado en 2011

Commentary: The affected sib-pair method in the context of an epidemiologic study design ⬇️

artículo científico publicado el 1 de enero de 1991

Commentary: contributions of epidemiology to the study of birth defects in humans.

artículo científico publicado en 1995

Commentary: epidemiology and the continuum from genetic research to genetic testing

scholarly article by Muin J. Khoury published 15 August 2002 in American Journal of Epidemiology

Commentary: facing the challenge of gene-environment interaction: the two-by-four table and beyond

artículo científico publicado en 2001

Communication of cancer-related genetic and genomic information: A landscape analysis of reviews

artículo científico publicado en 2018

Comparative effectiveness research and genomic medicine: an evolving partnership for 21st century medicine

scientific article published on October 2009

Comparative effectiveness research in cancer genomics and precision medicine: current landscape and future prospects

artículo científico publicado en 2013

Comparative effectiveness research in cancer: what has been funded and what knowledge gaps remain?

artículo científico publicado en 2013

Comparative epidemiology of selected midline congenital abnormalities

artículo científico publicado en 1994

Completeness of the Discharge Diagnoses as a Measure of Birth Defects Recorded in the Hospital Birth Record ⬇️

artículo científico publicado el 1 de julio de 1991

Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database

artículo científico publicado en 2012

Concepts and terms in genetic epidemiology: some similarities to infectious disease epidemiology

artículo científico publicado en 1988

Congenital malformations and intrauterine growth retardation: a population study.

artículo científico publicado en 1988

Contribution of Mendelian disorders to common chronic disease: opportunities for recognition, intervention, and prevention

artículo científico publicado en 2004

Contribution of birth defects and genetic diseases to pediatric hospitalizations. A population-based study

artículo científico publicado en 1997

Contribution of different HFE genotypes to iron overload disease: a pooled analysis

artículo científico publicado en 2000

Contribution of sickle cell disease to the occurrence of developmental disabilities: a population-based study.

artículo científico publicado en 2001

Convergence of Implementation Science, Precision Medicine, and the Learning Health Care System: A New Model for Biomedical Research

artículo científico publicado en 2016

Correction: A collaborative translational research framework for evaluating and implementing the appropriate use of human genome sequencing to improve health

article

Correspondence to Sand et al. “Critical Reappraisal of a Catechol-O-Methyltransferase Transversion Variant in Schizophrenia”

article by Christina M. Lill et al published April 2010 in Biological Psychiatry

Current Priorities for Public Health Practice in Addressing the Role of Human Genomics in Improving Population Health ⬇️

artículo científico publicado el 1 de abril de 2011

Current Social Media Conversations about Genetics and Genomics in Health: A Twitter-Based Analysis

article

D133P53, directly transactivated by p53, prevents p53-mediated apoptosis without inhibiting p53-mediated cell cycle arrest

artículo científico publicado en 2010

DNA banking for epidemiologic studies: a review of current practices

artículo científico publicado en 2002

Dealing with the evidence dilemma in genomics and personalized medicine

artículo científico publicado en 2010

Delta-aminolevulinic acid dehydratase genotype and lead toxicity: a HuGE review

artículo científico publicado en 2001

Deploying whole genome sequencing in clinical practice and public health: meeting the challenge one bin at a time

article

Descriptive epidemiology of holoprosencephaly and arhinencephaly in metropolitan Atlanta, 1968-1992.

artículo científico publicado en 1996

Descriptive epidemiology of small intestinal atresia, Atlanta, Georgia

artículo científico publicado en 1993

Detection of genotype-environment interaction in case-control studies of birth defects: how big a sample size?

artículo científico publicado en 1995

Developing Family Healthware, a family history screening tool to prevent common chronic diseases

scientific article published on 15 December 2008

Diabetes mellitus during pregnancy and the risks for specific birth defects: a population-based case-control study.

artículo científico publicado en 1990

Differences in the epidemiology of prematurity and intrauterine growth retardation

artículo científico publicado en 1986

Discriminative accuracy of genomic profiling comparing multiplicative and additive risk models

artículo científico publicado en 2010

Do we need genomic research for the prevention of common diseases with environmental causes?

artículo científico publicado en 2005

Does Periconceptional Multivitamin Use Reduce the Risk for Limb Deficiency in Offspring? ⬇️

artículo científico publicado el 1 de marzo de 1997

Does genetic testing really improve the prediction of future type 2 diabetes?

artículo científico publicado en 2006

Does light-to-moderate alcohol consumption during pregnancy increase the risk for renal anomalies among offspring?

artículo científico publicado en 1997

Does maternal cigarette smoking during pregnancy cause cleft lip and palate in offspring?

artículo científico

Does periconceptional multivitamin use reduce the risk of neural tube defects associated with other birth defects? data from two population-based case-control studies

artículo científico publicado en 1996

Early diagnosis of cystic fibrosis in the newborn period and risk of Pseudomonas aeruginosa acquisition in the first 10 years of life: A registry-based longitudinal study

artículo científico publicado en 2001

Ectopia cordis, midline defects and chromosome abnormalities: An epidemiologic perspective

Editorial: Emergence of Gene-Environment Interaction Analysis in Epidemiologic Research

artículo científico publicado en 2017

Effect of maternal and infant covariates on sibship correlation in birth weight

artículo científico publicado en 1988

Effect of prenatal diagnosis on epidemiologic studies of birth defects

artículo científico publicado en 2000

Elevated midtrimester serum methylmalonic acid levels as a risk factor for neural tube defects.

artículo científico publicado en 1995

Epidemiologic approaches to the use of DNA markers in the search for disease susceptibility genes

artículo científico

Epidemiologic evaluation of screening for risk factors: application to genetic screening.

artículo científico publicado en 1985

Epidemiological evaluation of the use of genetics to improve the predictive value of disease risk factors.

artículo científico publicado en 1995

Epidemiology matters: peering inside the "black box" in economic evaluations of genetic testing

artículo científico publicado en 2016

Epidemiology of biliary atresia: a population-based study

artículo científico publicado en 1997

Epidemiology of birth defects

artículo científico publicado en 1989

Epigenetic research in cancer epidemiology: trends, opportunities, and challenges

scientific article published on 10 December 2013

Estimating the contribution of genetic variants to difference in incidence of disease between population groups

artículo científico publicado en 2012

Etiologic heterogeneity of neural tube defects. II. Clues from family studies

artículo científico publicado en 1982

Etiologic heterogeneity of neural tube defects: clues from epidemiology

artículo científico publicado en 1982

Evaluating Precision Medicine’s Ability to Improve Population Health—Reply

scientific article published in The Journal of the American Medical Association

Evaluating the role of public health in implementation of genomics-related recommendations: a case study of hereditary cancers using the CDC Science Impact Framework

article

Evaluation of birth defect histories obtained through maternal interviews.

artículo científico publicado en 1990

Evaluation of family history as a risk factor and screening tool for detecting undiagnosed diabetes in a nationally representative survey population

artículo científico publicado en 2006

Evaluation of the Validity and Utility of Genetic Testing for Rare Diseases ⬇️

artículo científico publicado el 1 de enero de 2010

Evaluation of the discriminative accuracy of genomic profiling in the prediction of common complex diseases

artículo científico publicado en 2009

Evaluation of the potential excess of statistically significant findings in published genetic association studies: application to Alzheimer's disease

artículo científico publicado en 2008

Evidence Based Medicine and Big Genomic Data.

artículo científico publicado en 2018

Evidence synthesis and guideline development in genomic medicine: current status and future prospects

artículo científico publicado en 2015

Evidence-based classification of recommendations on use of genomic tests in clinical practice: dealing with insufficient evidence

artículo científico publicado en 2010

Evolution of the "drivers" of translational cancer epidemiology: analysis of funded grants and the literature

artículo científico publicado en 2015

Evolving Methods in Genetic Epidemiology. III. Gene-Environment Interaction in Epidemiologic Research ⬇️

artículo científico publicado el 1 de enero de 1997

Exogenous sex hormone exposure and the risk for VACTERL association

artículo científico publicado en 1986

Expanding the definition of a positive family history for early-onset coronary heart disease.

artículo científico publicado en 2006

Extending the reach of public health genomics: what should be the agenda for public health in an era of genome-based and “personalized” medicine?

artículo científico publicado en 2010

Extensions to methods of sib-pair linkage analyses ⬇️

artículo científico publicado el 1 de enero de 1991

Familial aggregation in chronic obstructive pulmonary disease: use of the loglinear model to analyze intermediate environmental and genetic risk factors

artículo científico publicado en 1985

Familial cancer history and chronic lymphocytic leukemia. A case-control study.

artículo científico publicado en 1989

Familial risk assessment for early-onset coronary heart disease.

artículo científico publicado en 2006

Familial spinocerebellar degeneration with corneal dystrophy

artículo científico publicado en 1985

Family history and personal genomics as tools for improving health in an era of evidence-based medicine

article

Family history and prevalence of diabetes in the U.S. population: the 6-year results from the National Health and Nutrition Examination Survey (1999-2004).

artículo científico publicado en 2007

Family history and prevalence of diabetes in the US population: 6-year results from the National Health and Nutrition Examination Survey (NHANES, 1999 2004)

article

Family history as a risk factor for early-onset stroke/transient ischemic attack among adults in the United States

artículo científico publicado en 2009

Family history assessment to detect increased risk for colorectal cancer: conceptual considerations and a preliminary economic analysis

artículo científico publicado en 2005

Family history in public health practice: a genomic tool for disease prevention and health promotion

artículo científico publicado en 2010

Family history of diabetes and prevalence of the metabolic syndrome in U.S. adults without diabetes: 6-year results from the National Health and Nutrition Examination Survey (1999-2004).

artículo científico publicado en 2009

Family history of heart disease and cardiovascular disease risk-reducing behaviors

artículo científico publicado en 2004

Family history of type 2 diabetes: A population-based screening tool for prevention?

article by Susan Hariri et al published February 2006 in Genetics in Medicine

Family history score as a predictor of breast cancer mortality: prospective data from the Cancer Prevention Study II, United States, 1982-1991.

artículo científico publicado en 1998

First-trimester anesthesia exposure and the risk of central nervous system defects: a population-based case-control study.

artículo científico publicado en 1994

From genes to public health: the applications of genetic technology in disease prevention. Genetics Working Group

artículo científico publicado en 1996

From genetics to genomics: using gene-based medicine to prevent disease and promote health in children

artículo científico publicado en 2005

From genomic medicine to precision medicine: highlights of 2015.

artículo científico publicado en 2016

From public health emergency to public health service: the implications of evolving criteria for newborn screening panels

artículo científico publicado en 2006

From public health genomics to precision public health: a 20-year journey

artículo científico publicado en 2017

Frontiers in cancer epidemiology: a challenge to the research community from the Epidemiology and Genomics Research Program at the National Cancer Institute

artículo científico publicado en 2012

Future health applications of genomics: priorities for communication, behavioral, and social sciences research

artículo científico publicado en 2010

GAPscreener: an automatic tool for screening human genetic association literature in PubMed using the support vector machine technique

artículo científico publicado en 2008

GWAS Integrator: a bioinformatics tool to explore human genetic associations reported in published genome-wide association studies

artículo científico publicado en 2011

Gene Prospector: an evidence gateway for evaluating potential susceptibility genes and interacting risk factors for human diseases

artículo científico publicado en 2008

Genetic Association Studies of Cancer: Where Do We Go from Here?

article by T. R. Rebbeck et al published 1 May 2007 in Cancer Epidemiology, Biomarkers & Prevention

Genetic Epidemiology and the Future of Disease Prevention and Public Health ⬇️

artículo científico publicado el 1 de enero de 1997

Genetic analysis of plasma sitosterol, apoprotein B, and lipoproteins in a large Amish pedigree with sitosterolemia

artículo científico publicado en 1986

Genetic associations with metabolic syndrome and its quantitative traits by race/ethnicity in the United States

artículo científico publicado en 2011

Genetic epidemiology with a capital E, ten years after

artículo científico

Genetic heterogeneity of prematurity and intrauterine growth retardation: clues from the Old Order Amish

artículo científico publicado en 1987

Genetic susceptibility to birth defects in humans: from gene discovery to public health action

artículo científico publicado en 2000

Genetic-environmental interactions in chronic airways obstruction

artículo científico publicado en 1986

Genetic-epidemiologic study of omphalocele and gastroschisis: evidence for heterogeneity

artículo científico publicado el 15 de noviembre de 1992

Genetics and genomics in practice: the continuum from genetic disease to genetic information in health and disease

artículo científico publicado en 2003

Genome Medicine: past, present and future ⬇️

artículo científico publicado el 31 de enero de 2011

Genome-wide association studies in pharmacogenomics: untapped potential for translation

artículo científico publicado en 2009

Genome-wide association studies, field synopses, and the development of the knowledge base on genetic variation and human diseases

artículo científico publicado en 2009

Genome-wide association studies, field synopses, and the development of the knowledge base on genetic variation and human diseases

Genomic profiling to promote a healthy lifestyle: not ready for prime time

artículo científico publicado en 2003

Genomics and public health at CDC.

artículo científico publicado en 2006

Genomics and public health in the United States: signposts on the translation highway

artículo científico publicado en 2006

Genomics in Public Health: Perspective from the Office of Public Health Genomics at the Centers for Disease Control and Prevention (CDC)

artículo científico publicado en 2015

Gestational age and intrauterine growth retardation among white and black very low birthweight infants: a population-based cohort study.

artículo científico publicado en 1994

HFE genotype and transferrin saturation in the United States

HLBS-PopOmics: an online knowledge base to accelerate dissemination and implementation of research advances in population genomics to reduce the burden of heart, lung, blood, and sleep disorders

artículo científico publicado en 2018

Harnessing the Angiogenic Potential of Stem Cell-Derived Exosomes for Vascular Regeneration

artículo científico publicado en 2016

Health beliefs among individuals at increased familial risk for type 2 diabetes: implications for prevention

artículo científico publicado en 2012

Health-related direct-to-consumer genetic tests: a public health assessment and analysis of practices related to Internet-based tests for risk of thrombosis

artículo científico publicado en 2008

Hemochromatosis-associated morbidity in the United States: an analysis of the National Hospital Discharge Survey, 1979-1997

artículo científico publicado en 2001

Hemochromatosis-associated mortality in the United States from 1979 to 1992: an analysis of Multiple-Cause Mortality Data

artículo científico publicado en 1998

Hereditary hemochromatosis: gene discovery and its implications for population-based screening

artículo científico publicado en 1998

Horizon scanning for new genomic tests ⬇️

artículo científico publicado el 1 de febrero de 2011

Horizon scanning for translational genomic research beyond bench to bedside

artículo científico publicado en 2014

How can polygenic inheritance be used in population screening for common diseases?

artículo científico publicado en 2013

How many genes underlie the occurrence of common complex diseases in the population?

artículo científico publicado en 2005

HuGE Watch: tracking trends and patterns of published studies of genetic association and human genome epidemiology in near-real time

artículo científico publicado en 2008

Human Genome Sequencing at the Population Scale: A Primer on High-Throughput DNA Sequencing and Analysis.

artículo científico publicado en 2017

Human teratogens, prenatal mortality, and selection bias.

artículo científico publicado en 1989

Imaging and counting threading dislocations in c-oriented epitaxial GaN layers

Impact of Violations and Deviations in Hardy-Weinberg Equilibrium on Postulated Gene-Disease Associations

article

Impact of prenatal diagnosis on the birth prevalence of neural tube defects, Atlanta, 1990-1991

Implementation of the 21-gene recurrence score test in the United States in 2011.

artículo científico

Implementing screening for Lynch syndrome among patients with newly diagnosed colorectal cancer: summary of a public health/clinical collaborative meeting

artículo científico publicado en 2011

Implications of Internet availability of genomic information for public health practice

artículo científico publicado en 2012

Implications of small effect sizes of individual genetic variants on the design and interpretation of genetic association studies of complex diseases.

artículo científico publicado en 2006

Improved ascertainment of cardiovascular malformations in infants with Down's syndrome, Atlanta, 1968 through 1989. Implications for the interpretation of increasing rates of cardiovascular malformations in surveillance systems

artículo científico publicado en 1992

Improvements in ability to detect undiagnosed diabetes by using information on family history among adults in the United States

artículo científico publicado en 2010

Improving the prediction of complex diseases by testing for multiple disease-susceptibility genes

artículo científico publicado en 2003

Improving validation practices in "omics" research

artículo científico publicado en 2011

Inbreeding and Diseases: Demographic, Genetic, and Epidemiologic Perspectives ⬇️

artículo científico publicado el 1 de enero de 1991

Inbreeding and prereproductive mortality in the Old Order Amish. I. Genealogic epidemiology of inbreeding

artículo científico publicado en 1987

Inbreeding and prereproductive mortality in the Old Order Amish. II. Genealogic epidemiology of prereproductive mortality

artículo científico publicado en 1987

Inbreeding and prereproductive mortality in the Old Order Amish. III. Direct and indirect effects of inbreeding

artículo científico publicado en 1987

Increased frequency of cystic fibrosis among infants with jejunoileal atresia

artículo científico publicado en 1998

Increased risk for familial ovarian cancer among Jewish women: a population-based case-control study.

artículo científico publicado en 1998

Increased risk for transverse digital deficiency after chorionic villus sampling: results of the United States Multistate Case-Control Study, 1988-1992

artículo científico publicado el 1 de enero de 1995

Increased risk of small intestinal atresia among twins in the United States.

artículo científico publicado en 1994

Increasing value and reducing waste in research design, conduct, and analysis

artículo científico publicado en 2014

Influence of arterial access sites and interventional procedures on vascular complications after cardiac catheterizations

artículo científico publicado el 1 de septiembre de 1992

Influence of familial risk on diabetes risk-reducing behaviors among U.S. adults without diabetes

artículo científico publicado en 2011

Informed consent for genetic research on stored tissue samples

artículo científico publicado en 1995

Informed consent for population-based research involving genetics

artículo científico publicado en 2001

Intention to analyze in pharmacogenomics studies

artículo científico publicado en 2008

Interaction between epidemiology and laboratory sciences in the study of birth defects: design of birth defects risk factor surveillance in metropolitan Atlanta

artículo científico publicado en 1993

Interaction of genetics and epidemiology in the literature

artículo científico publicado en 1986

Interface of genetics and epidemiology

artículo científico publicado en 2000

Interpretation of recurring weak associations obtained from epidemiologic studies of suspected human teratogens

article published in 1992

Invited commentary: from genome-wide association studies to gene-environment-wide interaction studies--challenges and opportunities

artículo científico publicado en 2008

Invited commentary: genes, environment, and hybrid vigor

article

Iron overload, public health, and genetics: evaluating the evidence for hemochromatosis screening

article

Is There Etiologic Heterogeneity between Upper and Lower Neural Tube Defects? ⬇️

artículo científico publicado el 15 de diciembre de 1992

Is family history a useful tool for detecting children at risk for diabetes and cardiovascular diseases? A public health perspective

artículo científico publicado en 2007

Is maternal obesity a risk factor for anencephaly and spina bifida?

artículo científico publicado en 1996

Khoury et al. Respond to "The Epicenter of Translational Science": Crossing All the T's

artículo científico publicado en 2010

Knowledge Integration in Cancer: Current Landscape and Future Prospects

artículo científico publicado en 2012

Knowledge gaps remain in the use of family health history in public health

article

Knowledge integration at the center of genomic medicine

artículo científico publicado en 2012

Letting the genome out of the bottle--will we get our wish?

artículo científico publicado en 2008

Leveraging Implementation Science to Address Health Disparities in Genomic Medicine: Examples from the Field

article

Leveraging biospecimen resources for discovery or validation of markers for early cancer detection

artículo científico publicado en 2015

Limb defects associated with major congenital anomalies: clinical and epidemiological study from the International Clearinghouse for Birth Defects Monitoring Systems

artículo científico publicado en 2000

Looking back at genomic medicine in 2011.

artículo científico publicado en 2012

Make it HuGE: human genome epidemiology reviews, population health, and the IJE

article

Maternal factors in cleft lip with or without palate: evidence from interracial crosses in the United States

artículo científico publicado en 1983

Maternal factors in dizygotic twinning: evidence from interracial crosses

artículo científico publicado en 1983

Maternal flu, fever, and the risk of neural tube defects: a population-based case-control study

artículo científico publicado en 1994

Maternal thyroid disease and risk of birth defects in offspring: a population-based case-control study.

artículo científico publicado en 1989

Medicine. Big data meets public health

artículo científico publicado en 2014

Medium chain acyl-CoA dehydrogenase deficiency human genome epidemiology review

artículo científico publicado en 1999

Mendelian randomisation: a new spin or real progress?

scientific article published on 01 September 2003

Mesenchymal stem cell-derived exosomes from different sources selectively promote neuritic outgrowth.

artículo científico publicado en 2016

Methimazole-induced myositis: a case report and review of the literature

artículo científico publicado en 2013

Minimum sample size estimation to detect gene-environment interaction in case-control designs

artículo científico publicado en 1994

Monitoring for congenital malformations

artículo científico publicado en 1986

Monitoring for multiple congenital anomalies: an international perspective

artículo científico publicado en 1994

Monitoring for new multiple congenital anomalies in the search for human teratogens

artículo científico publicado en 1993

Most published research findings are false-but a little replication goes a long way

artículo científico publicado en 2007

Multilevel research and the challenges of implementing genomic medicine

artículo científico publicado en 2012

Neural-tube defects

artículo científico publicado en 1999

No Shortcuts on the Long Road to Evidence-Based Genomic Medicine

article

Nontraditional epidemiologic approaches in the analysis of gene-environment interaction: case-control studies with no controls!

artículo científico publicado en 1996

O061: Impact of process control (PC) implementation and strategies to improve hand hygiene adherence (HHA), in device-associated infections (DAI) in an intensive care unit of adults (AICU).

artículo científico publicado en 2013

On the Use of Population Attributable Fraction to Determine Sample Size for Case-Control Studies of Gene-Environment Interaction

article

On the measurement and interpretation of birth defect associations in epidemiologic studies

artículo científico publicado en 1990

On the measurement of susceptibility in epidemiologic studies.

artículo científico publicado en 1989

On the measurement of susceptibility to genetic factors

artículo científico publicado en 1989

On the symmetry of limb deficiencies among children with multiple congenital anomalies

artículo científico publicado en 2001

On the synthesis and interpretation of consistent but weak gene-disease associations in the era of genome-wide association studies

artículo científico publicado en 2006

On the use of affected controls to address recall bias in case-control studies of birth defects.

artículo científico publicado en 1994

On the use of population attributable fraction to determine sample size for case-control studies of gene-environment interaction

artículo científico publicado en 2003

On the use of population-based registries in the clinical validation of genetic tests for disease susceptibility

artículo científico publicado en 2000

On the use of the term "syndrome" in clinical genetics and birth defects epidemiology

article

Opportunities and challenges for selected emerging technologies in cancer epidemiology: mitochondrial, epigenomic, metabolomic, and telomerase profiling

artículo científico publicado en 2012

Opportunities for translational epidemiology: the important role of observational studies to advance precision oncology

artículo científico publicado en 2015

PLoS Currents: Evidence on Genomic Tests – At the Crossroads of Translation ⬇️

artículo científico publicado el 2 de septiembre de 2010

Particle separation by external fields on periodic surfaces

Paternal effects on the human sex ratio at birth: evidence from interracial crosses.

artículo científico publicado en 1984

Patterns and trends of multiple congenital anomalies in birth defects surveillance systems

artículo científico publicado en 1991

Penetrance in the presence of genetic susceptibility to environmental factors ⬇️

artículo científico publicado el 1 de febrero de 1988

Periconceptional multivitamin use and the occurrence of conotruncal heart defects: results from a population-based, case-control study

artículo científico publicado en 1996

Personal utility and genomic information: look before you leap

artículo científico publicado en 2009

Phenopedia and Genopedia: disease-centered and gene-centered views of the evolving knowledge of human genetic associations

artículo científico publicado en 2009

Planning for the Future of Epidemiology in the Era of Big Data and Precision Medicine

artículo científico publicado en 2015

Polymorphisms of adrenergic receptors and the risk of heart failure

artículo científico publicado en 2003

Population and familial relative risks of disease associated with environmental factors in the presence of gene-environment interaction

article

Population sciences, translational research, and the opportunities and challenges for genomics to reduce the burden of cancer in the 21st century

artículo científico publicado en 2011

Population screening for genetic disorders in the 21st century: evidence, economics, and ethics

artículo científico publicado en 2009

Population screening in the age of genomic medicine

artículo científico publicado en 2003

Population study of congenital hypothyroidism and associated birth defects, Atlanta, 1979-1992 ⬇️

artículo científico publicado el 11 de julio de 1997

Population-based birth-defect and risk-factor surveillance: data from the Northern Netherlands

artículo científico publicado en 1996

Population-based precision cancer screening: a symposium on evidence, epidemiology, and next steps

journal article published in 2016

Population-based study of congenital heart defects in Down syndrome.

artículo científico publicado en 1998

Population-based study of the prevalence of family history of cancer: implications for cancer screening and prevention

scientific article published on September 2006

Potential increased risk of cancer from commonly used medications: an umbrella review of meta-analyses

artículo científico publicado en 2014

Precision Medicine vs Preventive Medicine

artículo científico publicado en 2019

Precision Public Health for the Era of Precision Medicine

artículo científico publicado en 2016

Preconceptional folate intake and malformations of the cardiac outflow tract. Baltimore-Washington Infant Study Group

artículo científico publicado en 1998

Predicting intrauterine growth retardation in sibships while considering maternal and infant covariates

artículo científico publicado en 1989

Predictive Analytics: Helping Guide the Implementation Research Agenda at the National Heart, Lung, and Blood Institute

artículo científico publicado en 2019

Predictive genetic testing for the identification of high-risk groups: a simulation study on the impact of predictive ability

artículo científico publicado en 2011

Predictive genetic testing for type 2 diabetes

artículo científico publicado en 2006

Pregnancy experience after delivery of a child with a major birth defect: a population study.

artículo científico publicado en 1995

Prevalence and Predictors of Cholesterol Screening, Awareness, and Statin Treatment Among US Adults With Familial Hypercholesterolemia or Other Forms of Severe Dyslipidemia (1999-2014)

Prevalence in the United States of selected candidate gene variants. Third National Health and Nutrition Examination Survey, 1991- 1994

artículo científico publicado en 2008

Prevalence of C282Y and H63D mutations in the hemochromatosis (HFE) gene in the United States

article

Prevalence of birth defects among low-birth-weight infants. A population study

artículo científico publicado en 1991

Prevalence, family history, and prevention of reported osteoporosis in U.S. women

artículo científico publicado en 2008

Primary immunodeficiency diseases: Practice among primary care providers and awareness among the general public, United States, 2008 ⬇️

artículo científico publicado el 1 de diciembre de 2010

Prioritizing genomic applications for action by level of evidence: a horizon-scanning method

artículo científico publicado en 2014

Prospective study of methylenetetrahydrofolate reductase (MTHFR) variant C677T and risk of all-cause and cardiovascular disease mortality among 6000 US adults

artículo científico publicado en 2012

Provocative questions in cancer epidemiology in a time of scientific innovation and budgetary constraints

artículo científico publicado en 2013

Public attitudes regarding the donation and storage of blood specimens for genetic research

artículo científico publicado en 2001

Public awareness and use of direct-to-consumer genetic tests: results from 3 state population-based surveys, 2006

Public awareness and use of direct-to-consumer personal genomic tests from four state population-based surveys, and implications for clinical and public health practice

artículo científico publicado en 2012

Public health action in genomics is now needed beyond newborn screening

artículo científico publicado en 2012

Public health genomics approach to type 2 diabetes

artículo científico publicado en 2008

Public health genomics: the end of the beginning

article

Public health genomics: translating obesity genomics research into population health benefits

artículo científico publicado en 2008

Public health impact of genetic tests at the end of the 20th century

article

Public knowledge regarding the role of genetic susceptibility to environmentally induced health conditions

article

Q&A: Muin Khoury on cancer epidemiology

artículo científico publicado en 2014

Quantifying the health benefits of genetic tests: the importance of a population perspective

artículo científico publicado en 2006

Quantitative analysis of associations between birth defects and suspected human teratogens ⬇️

artículo científico publicado el 15 de septiembre de 1991

Race-ethnic differences in the association of genetic loci with HbA1c levels and mortality in U.S. adults: the third National Health and Nutrition Examination Survey (NHANES III).

artículo científico publicado en 2012

Racial/ethnic differences in association of fasting glucose-associated genomic loci with fasting glucose, HOMA-B, and impaired fasting glucose in the U.S. adult population

artículo científico publicado en 2010

Recommendations and proposed guidelines for assessing the cumulative evidence on joint effects of genes and environments on cancer occurrence in humans

artículo científico publicado en 2012

Recommendations for returning genomic incidental findings? We need to talk!

artículo científico publicado en 2013

Recurrence of low birth weight in siblings

artículo científico publicado en 1989

Recurrence risk of neonatal hyperbilirubinemia in siblings.

artículo científico publicado en 1988

Recurrent pregnancy loss as an indicator for increased risk of birth defects: a population-based case-control study

artículo científico publicado en 1993

Reducing the burden of disease and death from familial hypercholesterolemia: a call to action

artículo científico publicado en 2014

Reduction of arthritis following intra-articular administration of an adeno-associated virus serotype 5 expressing a disease-inducible TNF-blocking agent

artículo científico publicado en 2007

Reply to Dr. Hook.

artículo científico publicado en 1990

Reply to Stephan et al.

artículo científico publicado en 2008

Reporting of human genome epidemiology (HuGE) association studies: an empirical assessment

artículo científico publicado en 2008

Reporting of systematic reviews: the challenge of genetic association studies

artículo científico publicado en 2007

Reporting, appraising, and integrating data on genotype prevalence and gene-disease associations

artículo científico publicado en 2002

Reproducible Research Practices and Transparency across the Biomedical Literature

artículo científico publicado en 2016

Required sample size and nonreplicability thresholds for heterogeneous genetic associations

artículo científico publicado en 2008

Research priorities for evaluating family history in the prevention of common chronic diseases

artículo científico publicado en 2003

Residential mobility during pregnancy: implications for environmental teratogenesis

artículo científico publicado en 1988

Revisiting the Clinical Validity of Multiplex Genetic Testing in Complex Diseases: Reply to Janssens et al.

artículo científico publicado en 2004

Right congenital diaphragmatic hernia a well-known pathology? ⬇️

artículo científico publicado el 15 de abril de 2003

Risk factors for trisomy 21: maternal cigarette smoking and oral contraceptive use in a population-based case-control study.

artículo científico publicado en 1999

Risk of childhood cancer for infants with birth defects. I. A record-linkage study, Atlanta, Georgia, 1968-1988.

artículo científico publicado en 1993

Risk of childhood cancer for infants with birth defects. II. A record-linkage study, Iowa, 1983-1989

artículo científico publicado en 1993

SEER cancer registry biospecimen research: yesterday and tomorrow

artículo científico publicado en 2014

STrengthening the REporting of Genetic Association Studies (STREGA)-an extension of the STROBE statement

article

STrengthening the REporting of Genetic Association Studies (STREGA): An Extension of the STROBE Statement

article

STrengthening the REporting of Genetic Association Studies (STREGA): an extension of the STROBE statement

artículo científico publicado en 2009

STrengthening the REporting of Genetic Association studies (STREGA)--an extension of the STROBE statement

scientific article published on April 2009

STrengthening the REporting of Genetic Association studies (STREGA)—an extension of the STROBE statement

article

Sample Size Requirements in Case-Only Designs to Detect Gene-Environment Interaction ⬇️

artículo científico publicado el 1 de noviembre de 1997

Sample size requirements to detect the effect of a group of genetic variants in case-control studies

artículo científico publicado en 2008

Sandhoff disease: a prevalent form of infantile GM2 gangliosidosis in Lebanon

artículo científico publicado en 1981

Scientific reporting is suboptimal for aspects that characterize genetic risk prediction studies: a review of published articles based on the Genetic RIsk Prediction Studies statement

artículo científico

Scope and strategies of genetic epidemiology: analysis of articles published in Genetic Epidemiology, 1984-1991

artículo científico publicado en 1993

Selected midline defect associations: a population study

Sensitivity, specificity, and positive predictive value of multiple malformations in isotretinoin embryopathy surveillance

artículo científico publicado en 1990

Size matters: just how big is BIG?: Quantifying realistic sample size requirements for human genome epidemiology

artículo científico publicado en 2009

Sodium and potassium intake and mortality among US adults: prospective data from the Third National Health and Nutrition Examination Survey

artículo científico publicado en 2011

Stakeholder assessment of the evidence for cancer genomic tests: insights from three case studies

artículo científico publicado en 2012

Steroid 5-{alpha}-reductase Type 2 (SRD5a2) gene polymorphisms and risk of prostate cancer: a HuGE review

artículo científico publicado en 2009

Strategies, actions, and outcomes of pilot state programs in public health genomics, 2003-2008.

artículo científico publicado en 2014

Strengthening the Reporting of Genetic Risk Prediction Studies: The GRIPS Statement

artículo científico publicado en 2011

Strengthening the reporting of Genetic RIsk Prediction Studies (GRIPS): explanation and elaboration

artículo científico publicado en 2011

Strengthening the reporting of Genetic RIsk Prediction Studies: the GRIPS Statement

artículo científico publicado en 2011

Strengthening the reporting of Genetic RIsk Prediction Studies: the GRIPS Statement

artículo científico publicado en 2011

Strengthening the reporting of Genetic Risk Prediction Studies: The GRIPS statement

artículo científico publicado en 2011

Strengthening the reporting of genetic association studies (STREGA): an extension of the STROBE Statement

article

Strengthening the reporting of genetic association studies (STREGA): an extension of the STROBE statement

article

Strengthening the reporting of genetic association studies (STREGA): an extension of the strengthening the reporting of observational studies in epidemiology (STROBE) statement

artículo científico publicado en 2009

Strengthening the reporting of genetic risk prediction studies (GRIPS): explanation and elaboration.

artículo científico publicado en 2011

Strengthening the reporting of genetic risk prediction studies (GRIPS): explanation and elaboration

artículo científico publicado en 2011

Strengthening the reporting of genetic risk prediction studies (GRIPS): explanation and elaboration

Strengthening the reporting of genetic risk prediction studies: The GRIPS Statement.

artículo científico publicado en 2011

Strengthening the reporting of genetic risk prediction studies: the GRIPS statement

Strengthening the reporting of genetic risk prediction studies: the GRIPS statement

Strengthening the reporting of genetic risk prediction studies: the GRIPS statement

artículo científico publicado en 2011

Strengthening the reporting of genetic risk prediction studies: the GRIPS statement.

artículo científico publicado en 2011

Strengthening the reporting of genetic risk prediction studies: the GRIPS statement.

artículo científico publicado en 2011

Survival of infants with spina bifida--Atlanta, 1972-1979.

artículo científico publicado en 1985

Synopsis of preterm birth genetic association studies: the preterm birth genetics knowledge base (PTBGene).

artículo científico publicado en 2010

Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database

artículo científico publicado en 2008

Systems-based candidate genes for human response to influenza infection

artículo científico publicado en 2009

Targeted Cancer Screening in Average-Risk Individuals

artículo científico publicado en 2015

Ten years of Genome Medicine

The Cancer Epidemiology Descriptive Cohort Database: A Tool to Support Population-Based Interdisciplinary Research

artículo científico publicado en 2016

The Cancer Genomics and Epidemiology Navigator: An NCI online tool to enhance cancer epidemiology research

artículo científico publicado en 2014

The Emergence of Networks in Human Genome Epidemiology

article

The Emergence of Translational Epidemiology: From Scientific Discovery to Population Health Impact ⬇️

artículo científico publicado el 5 de agosto de 2010

The Integration of Genomics into Public Health Research, Policy and Practice in the United States

article

The Scientific Foundation for personal genomics: recommendations from a National Institutes of Health-Centers for Disease Control and Prevention multidisciplinary workshop

artículo científico publicado en 2009

The arrival of genomic medicine to the clinic is only the beginning of the journey

artículo científico publicado en 2013

The association between family history of asthma and the prevalence of asthma among US adults: National Health and Nutrition Examination Survey, 1999-2004.

artículo científico publicado en 2009

The authors reply

The changing epidemiology of neural tube defects. United States, 1968-1989

artículo científico publicado el 1 de julio de 1992

The continuum of translation research in genomic medicine: how can we accelerate the appropriate integration of human genome discoveries into health care and disease prevention?

artículo científico publicado en 2007

The contribution of family history to the burden of diagnosed diabetes, undiagnosed diabetes, and prediabetes in the United States: analysis of the National Health and Nutrition Examination Survey, 2009-2014.

artículo científico publicado en 2018

The contribution of maternal epilepsy and its treatment to the etiology of oral clefts: a population based case-control study

artículo científico publicado en 1994

The current state of funded NIH grants in implementation science in genomic medicine: a portfolio analysis

artículo científico publicado en 2017

The emergence of biobanks: practical design considerations for large population-based studies of gene-environment interactions

article

The emergence of epidemiology in the genomics age.

artículo científico publicado en 2004

The emergence of networks in human genome epidemiology: challenges and opportunities

scholarly article published 18 December 2009

The epidemiologic approach to pharmacogenomics

artículo científico publicado en 2005

The evidence dilemma in genomic medicine

artículo científico publicado en 2008

The future of genetic studies of complex human diseases: an epidemiologic perspective

artículo científico publicado en 1998

The genomic applications in practice and prevention network

artículo científico publicado en 2009

The geometric increase in meta-analyses from China in the genomic era.

artículo científico publicado en 2013

The impact of early cystic fibrosis diagnosis on pulmonary function in children

scientific article published on 01 December 2002

The impact of genomics on public health practice: the case for change

artículo científico publicado en 2012

The impact of genotype frequencies on the clinical validity of genomic profiling for predicting common chronic diseases

artículo científico publicado en 2007

The integration of genomics into paediatric and perinatal epidemiology: guidelines for submitting human genome epidemiology (HuGE) reviews

artículo científico publicado en 2005

The interaction between dysmorphology and epidemiology: methodologic issues of lumping and splitting

artículo científico publicado en 1992

The interface of genetics and epidemiology

artículo científico publicado en 1986

The interface of genetics and public health: research and educational challenges

artículo científico publicado en 2000

The journey to personalized medicine

artículo científico publicado en 2005

The method of sib-pair linkage analysis in context of case-control design

artículo científico publicado en 1997

The multi-spectral line-polarization MSE system on Alcator C-Mod

artículo científico publicado en 2016

The need for a next-generation public health response to rare diseases

artículo científico publicado en 2016

The need for genetic variant naming standards in published abstracts of human genetic association studies

artículo científico publicado en 2009

The next generation of large-scale epidemiologic research: implications for training cancer epidemiologists

artículo científico publicado en 2014

The path from genome-based research to population health: development of an international public health genomics network

artículo científico publicado en 2006

The ponderal index in term newborn siblings

artículo científico publicado en 1990

The probiotic E. coli strain Nissle 1917 for the treatment of collagenous colitis: first results of an open-label trial

artículo científico publicado en 2004

The relation of computer-based measures of sperm morphology and motility to male infertility ⬇️

artículo científico publicado el 1 de mayo de 1992

The return of thalidomide: are birth defects surveillance systems ready?

artículo científico publicado en 1997

The role of genetic polymorphisms in environmental health

artículo científico publicado en 2003

The role of state public health agencies in genetics and disease prevention: results of a national survey

artículo científico publicado en 2001

The rules remain the same for genomic medicine: the case against "reverse genetic exceptionalism".

artículo científico publicado en 2010

The spectrum of congenital anomalies of the VATER association: An international study ⬇️

artículo científico publicado el 11 de julio de 1997

The surveillance of birth defects: the usefulness of the revised US standard birth certificate

scientific article published on 01 May 1996

The use of attributable fraction in the design and interpretation of epidemiologic studies.

artículo científico publicado en 1989

Tracking the epidemiology of human genes in the literature: the HuGE Published Literature database

artículo científico publicado en 2006

Transforming Epidemiology for 21st Century Medicine and Public Health

artículo científico publicado en 2013

Translational research in cancer genetics: the road less traveled

artículo científico publicado en 2009

Translational research is a key to nongeneticist physicians' genomics education

artículo científico publicado en 2014

Transmission disequilibrium test (TDT) when only one parent is available: the 1-TDT.

artículo científico publicado en 1999

Trends and outcomes after prenatal diagnosis of congenital cardiac malformations by fetal echocardiography in a well defined birth population, Atlanta, Georgia, 1990-1994.

artículo científico publicado en 1996

Trends and patterns of mortality associated with birth defects and genetic diseases in the United States, 1979–1992: An analysis of multiple-cause mortality data ⬇️

artículo científico publicado el 1 de enero de 1997

Trends in pharmacogenomic epidemiology: 2001-2007.

artículo científico publicado en 2009

Trends in postneonatal mortality in the United States. 1962 through 1978.

artículo científico publicado en 1984

Trends in published meta-analyses in cancer research, 2008-2013.

artículo científico publicado en 2016

Trends in rates of multiple vascular disruption defects, Atlanta, 1968-1989: is there evidence of a cocaine teratogenic epidemic?

artículo científico publicado el 1 de junio de 1992

Trends in utilization and costs of BRCA testing among women aged 18-64 years in the United States, 2003-2014.

artículo científico publicado en 2017

Using case-control designs for genome-wide screening for associations between genetic markers and disease susceptibility loci.

artículo científico publicado en 1999

Using deep learning to identify translational research in genomic medicine beyond bench to bedside

scholarly article by Yi-Yu Hsu et al published 1 January 2019 in Database

Using lifetime risk estimates in personal genomic profiles: estimation of uncertainty

artículo científico publicado en 2009

Using log-linear models to test for associations among congenital malformations

artículo científico publicado en 1991

Utility before business

artículo científico publicado en 2014

Utilization of epidermal growth factor receptor (EGFR) testing in the United States: a case study of T3 translational research

artículo científico publicado en 2013

Vitamin A and cardiac outflow tract defects

artículo científico publicado en 2001

What is the clinical utility of genetic testing?

artículo científico publicado en 2006

What is translational genomics? An expanded research agenda for improving individual and population health

artículo científico publicado en 2014

Why Hasn't Genomic Testing Changed the Landscape in Clinical Oncology?

artículo científico publicado en 2012

Why should genomic medicine become more evidence-based?

artículo científico publicado en 2007

Will genomics widen or help heal the schism between medicine and public health?

artículo científico publicado en 2007

msJAMA. The role of genomics in public health and disease prevention

article

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